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    首頁 > 產(chǎn)品中心 > 生化試劑 > 小分子化合物 > abs47027913Mecamylamine hydrochloride 826-39-1

    Mecamylamine hydrochloride 826-39-1

    簡要描述:Mecamylamine hydrochloride 826-39-1
    Mecamylamine hydrochloride is an orally active, nonselective, noncompetitive nAChR antagonist that can treat various neuropsychiatric disorders.

    • 產(chǎn)品型號:abs47027913
    • 廠商性質(zhì):生產(chǎn)廠家
    • 更新時間:2026-01-07
    • 訪  問  量:554

    詳細介紹

    品牌absinCAS826-39-1
    分子式C11H22ClN純度98%
    分子量203.75貨號abs47027913
    規(guī)格1mg供貨周期現(xiàn)貨
    主要用途is an orally active應用領域化工,生物產(chǎn)業(yè),農(nóng)林牧漁,制藥/生物制藥,綜合

    Mecamylamine hydrochloride 826-39-1

    產(chǎn)品描述
    描述
    Mecamylamine hydrochloride is an orally active, nonselective, noncompetitive nAChR antagonist that can treat various neuropsychiatric disorders. Mecamylamine hydrochloride is originally used as a ganglionic blocker in treating hypertension. Mecamylamine hydrochloride can easily crosses the blood-brain barrier.
    純度
    98%
    儲存/保存方法
    Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
    基本信息
    別名
    鹽酸美加明
    外觀
    White crystalline powder
    可溶性/溶解性
    DMSO : 31.25 mg/mL (153.37 mM; Need ultrasonic)
    生物活性
    靶點
    nAChR
    In vitro(體外研究)
    Mecamylamine blocks muscle nAChRs in a use- and voltagedependent manner. Mecamylamine blocks the nicotinic currents via trapping mechanism. The main feature of this block is the phenomenon of block relief, which might be revealed by combined action of depolarization and activation of nAChRs. The experimental study of the Mecamylamine action on muscle nAChRs revealed that: (1) Mecamylamine (1-20 μM) reduces evoked end-plate currents (EPC) amplitude with Hill’s constant equal to 1.2 and IC50 = 7.8 μM at holding potential –70 mV; (2) the calculated depth of its interaction with the muscle nAChR channel is almost half of the one of neuronal nAChRs (0.37 compare to 0.72 for neuronal nAChRs); (3) simultaneous membrane depolarization and repetitive activation of postsynaptic nAChRs by motor nerve stimulation produced rapid block relief dependent on the degree of depolarization, number of conditioning signals and Mecamylamine concentration, and only slightly depended on the rate of stimulation.
    In vivo(體內(nèi)研究)
    Mecamylamine (0.5-1 mg/kg; Intraperitoneal injection; C57BL/6J mice) has antidepressant-like effects in both the TST and FST and these effects are dependent on bothβ2 andα7 subunits.
    研究領域
    研究領域
    Cardiovascular
    Drug DiscoverySmall Molecule DrugLead Compound Discovery
    Mecamylamine hydrochloride 826-39-1溫馨提示:本產(chǎn)品僅作科研實驗使用,不支持臨床等研究

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